Variant report

Variant	rs73472268
Chromosome Location	chr7:147810479-147810480
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs10233900	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1813148	chr7:147796154-147837213	Enhancers Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:147801800-147813400	Weak transcription	Brain Angular Gyrus	brain
2	chr7:147805200-147814200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:147805200-147815400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr7:147805200-147817000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr7:147805600-147812200	Weak transcription	Brain Substantia Nigra	brain
6	chr7:147805800-147812400	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr7:147807800-147814200	Weak transcription	Fetal Intestine Large	intestine
8	chr7:147807800-147814400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:147807800-147815400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr7:147807800-147815800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:147810000-147812200	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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